chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155164915851649159TG18INTERGENIChomozygous48307437
155165059551650596CCA15INTERGENIChomozygous48307442
155165526851655269CT11INTERGENICheterozygous48307453
155167861151678612TC19INTERGENICheterozygous48307496
155168336151683362GGT29INTERGENIChomozygous48307508
155169090451690905GGA8GENICheterozygous48307526
155169090551690906A-8GENICpossibly homozygous48307527
155169555051695551AAG16GENIChomozygous48307543
155166655551666559AAAG----5INTERGENIChomozygous48601777
155168554551685547AC--18INTERGENICheterozygous48601779
155168647251686476GTGT----6INTERGENICheterozygous48601781
155170169651701697A-18GENICheterozygous48601783
155169074351690745AC--6GENIChomozygous48506492
155170632651706327CCT13INTERGENIChomozygous48307574
155170634951706350G-10INTERGENICpossibly homozygous48307575
155170638351706384GA9INTERGENIChomozygous48307576
155170643151706432CA10INTERGENIChomozygous48307577
155170646051706463AGG---11INTERGENIChomozygous48307578
155171751851717519A-17INTERGENIChomozygous48307599
155171877151718772TC50INTERGENICheterozygous48307602
155172101651721017CA20INTERGENICheterozygous48307606
155172227151722285AATTGATAAATAGG--------------6INTERGENIChomozygous48307607
155172368151723683GT--13INTERGENICheterozygous48506504
155172960551729606TG29INTERGENICheterozygous48671818